Manufacturing Operator I

Katalyst CRO; Portsmouth (NH); On-site; USD 42,000 - 60,000; Full time

Job summary

Katalyst CRO in Portsmouth, NH is seeking a Manufacturing Support Associate to help keep cGMP suites stocked, clean, and ready for production. You will prepare materials, autoclave items, and assist with equipment maintenance while following GMP and aseptic practices.

The role emphasizes attention to detail, teamwork, and strict documentation of SOPs and GDPs. Candidates with 2 years in pharma/biotech manufacturing and a life sciences degree are encouraged to apply.

Qualifications

• Basic cGMP knowledge.
• Aseptic technique awareness.
• SOP & documentation (GDP) understanding.
• Attention to detail and teamwork.

Responsibilities

• Perform daily 6S, stocking, and cleaning of suites and parts.
• Prepare, assemble, and autoclave materials for production.
• Handle material movement across production areas.
• Perform routine equipment maintenance and cleaning.
• Complete weekly/monthly cleaning (e.g., inoculum rooms).
• Maintain GMP/GDP-compliant documentation.
• Follow aseptic techniques and contamination control practices.
• Support training, meetings, and assigned tasks.

Skills

cGMP knowledge

Aseptic technique

SOP documentation

Attention to detail

Teamwork

Education

Bachelor's in Life Sciences / Biotechnology / related field

Job description

Job Description

Supports cGMP manufacturing suites by ensuring proper stocking, cleaning, material preparation, and equipment maintenance while following GMP and aseptic practices.

Job Description

Supports cGMP manufacturing suites by ensuring proper stocking, cleaning, material preparation, and equipment maintenance while following GMP and aseptic practices.

Responsibilities

• Perform daily 6S, stocking, and cleaning of suites and parts.
• Prepare, assemble, and autoclave materials for production.
• Handle material movement across production areas.
• Perform routine equipment maintenance and cleaning.
• Complete weekly/monthly cleaning (e.g., inoculum rooms).
• Maintain GMP/GDP-compliant documentation.
• Follow aseptic techniques and contamination control practices.
• Support training, meetings, and assigned tasks

Requirements

• 02 years in pharma/biotech/manufacturing (freshers with relevant exposure can apply).
• Bachelor's in Life Sciences / Biotechnology / related field.

Mandatory Requirements

• Basic cGMP knowledge.
• Aseptic technique awareness.
• SOP & documentation (GDP) understanding.
• Attention to detail and teamwork.